These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 31004034)

  • 21. Readthrough of SCN5A Nonsense Mutations p.R1623X and p.S1812X Questions Gene-therapy in Brugada Syndrome.
    Teng S; Huang J; Gao Z; Hao J; Yang Y; Zhang S; Pu J; Hui R; Wu Y; Fan Z
    Curr Gene Ther; 2017; 17(1):50-58. PubMed ID: 28552050
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Hemophilia Gene Therapy: Ready for Prime Time?
    VandenDriessche T; Chuah MK
    Hum Gene Ther; 2017 Nov; 28(11):1013-1023. PubMed ID: 28793786
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The multifactorial etiology of inhibitor development in hemophilia: genetics and environment.
    Gouw SC; van den Berg HM
    Semin Thromb Hemost; 2009 Nov; 35(8):723-34. PubMed ID: 20169509
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX gene.
    Wulff K; Bykowska K; Lopaciuk S; Herrmann FH
    Acta Biochim Pol; 1999; 46(3):721-6. PubMed ID: 10698280
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Increased bone resorption in hemophilia.
    Rodriguez-Merchan EC; Valentino LA
    Blood Rev; 2019 Jan; 33():6-10. PubMed ID: 29857920
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mutation characteristic of 103 haemophilia A patients in Vietnam: Identification of novel mutations.
    Luu DV; Tran TH; Nguyen DH; Luong LH; Bui HTT; Nguyen MT; Ta MH; Tran VK; Bui TH; Ta TV
    Haemophilia; 2019 Jul; 25(4):e274-e277. PubMed ID: 30913330
    [No Abstract]   [Full Text] [Related]  

  • 27. The Canadian "National Program for hemophilia mutation testing" database: a ten-year review.
    Rydz N; Leggo J; Tinlin S; James P; Lillicrap D
    Am J Hematol; 2013 Dec; 88(12):1030-4. PubMed ID: 23913812
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A de novo factor VIII mutation in a haemophilia B family leading to combined deficiency of factor VIII and IX.
    Prabhudesai A; Shanbhag S; Mirgal D; Kawankar N; Shetty S
    Haemophilia; 2017 Sep; 23(5):e477-e479. PubMed ID: 28750473
    [No Abstract]   [Full Text] [Related]  

  • 29. Molecular basis of hemophilia.
    Lozier JN; High KA
    Hematol Pathol; 1990; 4(1):1-26. PubMed ID: 2111315
    [No Abstract]   [Full Text] [Related]  

  • 30. Strategies against Nonsense: Oxadiazoles as Translational Readthrough-Inducing Drugs (TRIDs).
    Campofelice A; Lentini L; Di Leonardo A; Melfi R; Tutone M; Pace A; Pibiri I
    Int J Mol Sci; 2019 Jul; 20(13):. PubMed ID: 31284579
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Deficiencies in factors IX and VIII: what is now known.
    Kurachi K; Yao SN; Furukawa M; Kurachi S
    Hosp Pract (Off Ed); 1992 Feb; 27(2):41-51. PubMed ID: 1735764
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [The molecular genetics of hemophilia].
    Yoshitake S
    Tanpakushitsu Kakusan Koso; 1986 Oct; 31(13):1301-18. PubMed ID: 3101138
    [No Abstract]   [Full Text] [Related]  

  • 33. [Structure and function of factor VIII and factor IX gene and molecular DNA diagnosis in hemophilia A and B].
    Herrmann FH; Wehnert M; Wulff K
    Z Arztl Fortbild (Jena); 1988; 82(22):1116-22. PubMed ID: 2907834
    [No Abstract]   [Full Text] [Related]  

  • 34. Premature termination codon readthrough in human cells occurs in novel cytoplasmic foci and requires UPF proteins.
    Jia J; Werkmeister E; Gonzalez-Hilarion S; Leroy C; Gruenert DC; Lafont F; Tulasne D; Lejeune F
    J Cell Sci; 2017 Sep; 130(18):3009-3022. PubMed ID: 28743738
    [TBL] [Abstract][Full Text] [Related]  

  • 35. DNA polymorphisms for carrier detection of hemophilia in Thailand.
    Chuansumrit A; Goodeve A; Sasanakul W; Peake IR; Pintadit P; Hathirat P; Preston FE; Isarangkul P
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():201-6. PubMed ID: 8629107
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Status of gene transfer for hemophilia A and B.
    Thompson AR
    Thromb Haemost; 1991 Jul; 66(1):119-22. PubMed ID: 1926041
    [No Abstract]   [Full Text] [Related]  

  • 37. Gene therapy for hemophilia: the clot thickens.
    High KA
    Hum Gene Ther; 2014 Nov; 25(11):915-22. PubMed ID: 25397928
    [No Abstract]   [Full Text] [Related]  

  • 38. [Molecular genetics of hemophilia A].
    De Brasi CD; Slavutsky IR; Larripa IB
    Medicina (B Aires); 1996; 56(5 Pt 1):509-17. PubMed ID: 9239887
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Genetic diagnosis in haemophiliacs (haemophilia A, B, carrier)].
    Mikami S
    Rinsho Byori; 1990 Jun; Suppl 85():102-13. PubMed ID: 1976834
    [No Abstract]   [Full Text] [Related]  

  • 40. Mutation analysis in 51 patients with haemophilia A: report of 10 novel mutations and correlations between genotype and clinical phenotype.
    Hill M; Deam S; Gordon B; Dolan G
    Haemophilia; 2005 Mar; 11(2):133-41. PubMed ID: 15810915
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.